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Neue genetische Ursache für Glasknochen-Krankheit entdeckt –...
www.innovations-report.de
Jutta Becker , Oliver Semler , Christian Gilissen , Yun Li , Hanno Jörn Bolz , Cecilia Giunta , Carsten Bergmann , Marianne Rohrbach ...
Forscher der Uniklinik Köln entdecken neues Gen und Pathomechanismus...
www.uni-protokolle.de
· PD Dr. Hanno Jörn Bolz Institut für Humangenetik der Uniklinik Köln (jetzt am Zentrum für Humangenetik, Bioscientia, Ingelheim)
Bild.de: Neue Elbfähre „liinsand“ nach zwei Wochen Testbetrieb gestartet:...
Kapitän Jörn Bolz (52) auf der Fähren-Brücke kennt die Strecke gut – er pendelte früher auf dem Katamaran „Hansestar“ (wurde
Kooperation mit neuem Zentrum für Humangenetik in Frankfurt -...
www.buergerhospital-ffm.de
Dr. med. Hanno Jörn Bolz. Er und sein Team aus Ärzten und Wissenschaftlern unterstützen ihre Patienten und deren Familien u. a. dabei, ...
Netzwerk-Profile
Jörn Bolz - Stade, Grünendeich (Seefahrtschule Grünendeich)
www.stayfriends.de
Jörn Bolz ist Mitglied bei StayFriends und hat bis diese Schule besucht: Seefahrtschule Grünendeich.
Facebook: Jörn Bolz Profile | Facebook
Profile der Personen mit dem Namen Jörn Bolz auf Facebook anzeigen Tritt Facebook bei, um dich mit Jörn Bolz und anderen Nutzern, die du vielleicht kennst, ...
Hanno Jörn Bolz - Loop - Frontiersloop.frontiersin.org › people › bio
loop.frontiersin.org
Genetics. dystrophy. Child health (paediatrics). spinocerebellar ataxia. β-III spectrin. SCA5. SPTBN2. DNA Mutational Analysis. Eye Proteins. Genes, Recessive.
Bücher
Search | IOVS | ARVO Journals
iovs.arvojournals.org
Hanno Joern Bolz; Raoul Heller; Michaela Thoenes; Gudrun Nürnberg; Peter Nürnberg; Srikanth Karnati; Daniel Swan; Eveline Baumgart-Vogt; Maha Zaki.
Molecular Vision: Articles by the Authors
www.molvis.org
Articles by Christian Becker · Articles by Erika Wegscheider · Articles by Gudrun Nürnberg · Articles by Peter Nürnberg · Articles by Hanno Jörn Bolz · Articles by ...
OPUS Würzburg | Suchen
opus.bibliothek.uni-wuerzburg.de
U5 Tri-snRNP Integration and Is Associated with Retinitis Pigmentosa (2014); Bastian Linder Anja Hirmer Andreas Gal Klaus Rüther Hanno Jörn Bolz Christoph ...
Diagnostic applications of next generation sequencing: working...
www.degruyter.com
... Andrea Gehring , Carsten Bergmann , Hanno Jörn Bolz , Manfred Stuhrmann , Saskia Biskup , Klaus H. Metzeler and Hanns-Georg Klein.
Dokumente zum Namen
SCHATTENBLICK - GENETIK/389: Neue genetische Ursache für...
www.schattenblick.de
Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno Jörn Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike ...
[PDF] Curriculum vitae: Prof. Dr. Hanno Jörn Bolz, MD - Free Download...
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Download Curriculum vitae: Prof. Dr. Hanno Jörn Bolz, MD...
Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type...
www.scienceopen.com
Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type Ca2+ channels. Authors: Jörg Striessnig, Hanno Jörn Bolz,, Alexandra ...
Extended mutation spectrum of Usher syndrome in Finland. – ScienceOpen
www.scienceopen.com
Authors: Hanna Västinsalo, Reetta Jalkanen, Carsten Bergmann, Christine Neuhaus, Leenamaija Kleemola, Liisa Jauhola, Hanno Jörn Bolz, Eeva-Marja ...
Wissenschaftliche Veröffentlichungen
DFG - GEPRIS - Privatdozent Dr. Hanno Jörn Bolz
gepris.dfg.de
Privatdozent Dr. Hanno Jörn Bolz, Institut für GenetikKöln
How did darcy pohland diego
xuxpusva.ga
Bernhard Friedrich Peter,; Darcy Lidington,; Aki Harada,; Hanno Jörn Bolz,; Lukas Vogel,; Scott Heximer,; Sarah Spiegel,; Ulrich Pohl, and; Steffen-Sebastian .
Privatdozent Dr. Hanno Jörn Bolz - Gepris - DFG
gepris.dfg.de
Privatdozent Dr. Hanno Jörn Bolz. As Former applicant. Completed projects. Klonierung und Charakterisierung eines neuen Gens für das Usher-Syndrom Typ
Identification of a PRPF4 Loss-of-Function OPUS Würzburgopus.bibliothek.uni-wuerzburg.de › ...
opus.bibliothek.uni-wuerzburg.de
Bastian Linder, Anja Hirmer, Andreas Gal, Klaus Rüther, Hanno Jörn Bolz, Christoph Winkler, Bernhard Laggerbauer, Utz Fischer. Pre-mRNA ...
Veröffentlichungen allgemein
Publications Authored by Hanno Joern Bolz | PubFacts
www.pubfacts.com
Publications Authored by Hanno Joern Bolz
Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage-gated L-type...
link.springer.com
Voltage-gated Ca2+ channels couple membrane depolarization to Ca2+-dependent intracellular signaling events. This is achieved by mediating Ca2+ ion influx
Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling...
www.biomedsearch.com
... Nürnberg; Hanswalter Zentgraf; Friederike Koerber; Klaus Addicks; Ezzat Elsobky; Thomas Benzing; Bernhard Schermer; Hanno Jörn Bolz.
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and...
www.wikidata.org
scientific article
Artikel & Meinungen
Channelpedia - EPFLchannelpedia.epfl.ch › references
channelpedia.epfl.ch
Authors: Jörg Striessnig, Hanno Jörn Bolz, Alexandra Koschak. Journal, date & volume: , Mar 7 , ,. PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/ ...
Sonstiges
Exome Sequencing Identifies Truncating Mutations in Human SERPINF1 in...
slideplayer.com
... Human SERPINF1 in Autosomal- Recessive Osteogenesis Imperfecta Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno Jörn Bolz, Cecilia Giunta, ...
Hanno Joern Bolz (born February 3, 1970), German geneticist,...
prabook.com
Hanno Joern Bolz, German geneticist, researcher. Achievements include discovery of identification of Cadherin-23 as the gene defective in Usher syndrome type...
Projektbericht: Identifizierung neuer Krankheitsgene für isolierte...
docplayer.org
Projektbericht: Identifizierung neuer Krankheitsgene für isolierte und syndromale Retinopathien Prof. Dr. med. Hanno Jörn Bolz EXPOSEE Im Folgenden fasse ich die ...
GMS | 29. Wissenschaftliche Jahrestagung der Deutschen Gesellschaft...
www.egms.de
Authors Hanno Jörn Bolz - Bioscientia Center for Human Genetics, Ingelheim, Germany; Institut für Humangenetik, Universitätsklinikum Köln
Channelopathies in Cav1.1, Cav1.3, and Cav1.4 voltage ...cyberleninka.org › article
cyberleninka.org
Jörg Striessnig • Hanno Jörn Bolz • Alexandra Koschak. Received: 27 January Revised: 3 February Accepted: 5 February Published online:
Characterization of the deletion breakpoint in patient 2557figshare.com › articles › Characterization_of_the_deleti...
figshare.com
... Ulrike Orth Christian Becker Erika Wegscheider Gudrun Nürnberg Peter Nürnberg Hanno Jörn Bolz Andreas Gal Wolfgang Berger.
Compound heterozygous BRAT1 mutations cause familial ...read.qxmd.com › read › compoun...
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Ghada Abdel-Salam, Michaela Thoenes, Hanan H Afifi, Friederike Körber, Daniel Swan, Hanno Jörn Bolz Orphanet Journal of Rare Diseases 2014, 9: 12.
Biblioteca Digital UniRedentor
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Altmetric – Exome Sequencing Identifies Truncating Mutations in Human...
www.altmetric.com
Jutta Becker, Oliver Semler, Christian Gilissen, Yun Li, Hanno Jörn Bolz, Cecilia Giunta, Carsten Bergmann, Marianne Rohrbach, Friederike Koerber, Katharina ...
CiteSeerX — ION CHANNELS, RECEPTORS AND TRANSPORTERS
citeseerx.ist.psu.edu
@MISC{Striessnig_ionchannels,, author = {Jörg Striessnig and Hanno Jörn Bolz and Ra Koschak and J. Striessnig and A. Koschak and H. J. Bolz and H. J. Bolz} ...
Extended mutation spectrum of Usher syndrome in Finland —...
researchportal.helsinki.fi
Hanna Västinsalo, Reetta Jalkanen, Christine Neuhaus, Leenamaija Kleemola, Liisa Jauhola, Hanno Jörn Bolz, Eeva-Marja Sankila · Haartman Institute ...
Gendefekt verursacht neues Syndrom - Forscher der Uniklinik ...medizin-aspekte.de › gendefekt-verursacht-neues-syndr...
medizin-aspekte.de
PD Dr. Hanno Jörn Bolz Institut für Humangenetik der Uniklinik Köln (Jetzt am Zentrum für Humangenetik, Bioscientia, Ingelheim)
Dr. med. Dieter Schäfer in Frankfurt am Main FA für...
www.aerzte.de
➤ Dr. med. Dieter Schäfer in Frankfurt am Main FA für Humangenetik ➤ Bewertungen, Leistungen, Telefonnummern, Öffnungszeiten, Online Wunsch-Termin ➤...
Identification of a PRPF4 Loss-of-Function Variant That Abrogates...
journals.plos.org
Hanno Jörn Bolz,. Affiliations Institute of Human Genetics, University Hospital of Cologne, Cologne, Germany, Bioscientia Center for Human ...
JCI - Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog...
www.jci.org
Claudia Dafinger ... Bernhard Schermer, Hanno Jörn Bolz. Claudia Dafinger ... Bernhard Schermer, Hanno Jörn Bolz. Published July 1, Citation ...
CiteSeerX — Regulation of Resistance Artery Tone
citeseerx.ist.psu.edu
by Bernhard Friedrich Peter , Darcy Lidington , Aki Harada , Hanno Jörn Bolz , Lukas Vogel , Sarah Spiegel , Ulrich Pohl , Steffen-sebastian Bolz , Bernhard ...
Researchers discover novel gene and new pathomechanism for Joubert...
medizin-aspekte.de
Contact: PD Dr. Hanno Jörn Bolz Institute of Human Genetics, University Hospital of Cologne, Germany (currently at the Bioscientia Center for Human Genetics, ...
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and...
www.infona.pl
... Markus M Hess, Andreas Gal, Tobias Eisenberger, Carsten Bergmann, Gudrun Nürnberg, Peter Nürnberg, Karen P Steel, Marlies Knipper, Hanno Jörn Bolz.
Targeted next-generation sequencing identifies a homozygous nonsense...
read.qxmd.com
... Mansour, Markus Nauck, Gudrun Nürnberg, Peter Nürnberg, Christian Decker, Claudia Dafinger, Inga Ebermann, Carsten Bergmann, Hanno Jörn Bolz.
The arginine residue at position 192 is essential for integration of...
figshare.com
The arginine residue at position 192 is essential for integration of PRPF4 into snRNPs.
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